JP2018535995A - 癌を治療するためのピリミド−ピリダジノンの使用 - Google Patents
癌を治療するためのピリミド−ピリダジノンの使用 Download PDFInfo
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- JP2018535995A JP2018535995A JP2018528583A JP2018528583A JP2018535995A JP 2018535995 A JP2018535995 A JP 2018535995A JP 2018528583 A JP2018528583 A JP 2018528583A JP 2018528583 A JP2018528583 A JP 2018528583A JP 2018535995 A JP2018535995 A JP 2018535995A
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- Prior art keywords
- amino
- pyridazin
- phenyl
- oxo
- dihydropyrimido
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- 206010028980 Neoplasm Diseases 0.000 title claims abstract description 92
- 201000011510 cancer Diseases 0.000 title claims abstract description 52
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- 150000001875 compounds Chemical class 0.000 claims abstract description 60
- 238000000034 method Methods 0.000 claims abstract description 52
- 150000003839 salts Chemical class 0.000 claims abstract description 11
- 230000004614 tumor growth Effects 0.000 claims abstract description 11
- 150000002148 esters Chemical class 0.000 claims abstract description 10
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 9
- 238000000338 in vitro Methods 0.000 claims abstract description 6
- 238000001727 in vivo Methods 0.000 claims abstract description 5
- -1 4- (piperazin-1-ylmethyl) phenylamino Chemical group 0.000 claims description 91
- 125000000623 heterocyclic group Chemical group 0.000 claims description 72
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 47
- 229910052799 carbon Inorganic materials 0.000 claims description 38
- 125000003118 aryl group Chemical group 0.000 claims description 33
- 125000001072 heteroaryl group Chemical group 0.000 claims description 33
- 210000004027 cell Anatomy 0.000 claims description 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims description 18
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- 125000002950 monocyclic group Chemical group 0.000 claims description 12
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
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- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 208000025205 Mantle-Cell Lymphoma Diseases 0.000 claims description 6
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
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- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 4
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 241000124008 Mammalia Species 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- 208000031637 Erythroblastic Acute Leukemia Diseases 0.000 claims description 3
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- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 3
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- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 2
- 206010005003 Bladder cancer Diseases 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 2
- 208000029742 colonic neoplasm Diseases 0.000 claims description 2
- 208000020816 lung neoplasm Diseases 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 201000005112 urinary bladder cancer Diseases 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 6
- TUCUGMSPHGMPOI-UHFFFAOYSA-N 6h-pyrimido[4,5-d]pyridazin-5-one Chemical compound C1=NC=C2C(=O)NN=CC2=N1 TUCUGMSPHGMPOI-UHFFFAOYSA-N 0.000 claims 3
- ITZWDHUUXWCUHN-UHFFFAOYSA-N OC(=O)CC1CCC(CC1)c1ccc(NC2NC(NC3CNNC(=O)C23)N2CCCCCC2)cc1 Chemical compound OC(=O)CC1CCC(CC1)c1ccc(NC2NC(NC3CNNC(=O)C23)N2CCCCCC2)cc1 ITZWDHUUXWCUHN-UHFFFAOYSA-N 0.000 claims 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 3
- ZLJJGDNOJCDNKD-UHFFFAOYSA-N 2-[1-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-3-yl]acetic acid Chemical compound C1C(CC(=O)O)CCCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 ZLJJGDNOJCDNKD-UHFFFAOYSA-N 0.000 claims 2
- JHCFYMYSDATETA-UHFFFAOYSA-N 2-[1-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCCCCC2)=NC=1NC(C=C1)=CC=C1N1CCC(CC#N)CC1 JHCFYMYSDATETA-UHFFFAOYSA-N 0.000 claims 2
- BDIYBAQRVGMTLJ-UHFFFAOYSA-N 2-[1-[5-[[2-[4-(cyanomethyl)piperidin-1-yl]-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]pyridin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=N1)=CC=C1N1CCC(CC#N)CC1 BDIYBAQRVGMTLJ-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 2
- 235000011054 acetic acid Nutrition 0.000 claims 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 2
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 claims 2
- 125000004526 pyridazin-2-yl group Chemical group N1N(C=CC=C1)* 0.000 claims 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 claims 1
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 claims 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims 1
- CQYPQRMXAKUQDG-UHFFFAOYSA-N 1-[4-[(5-oxo-2-phenyl-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperidine-4-carboxylic acid Chemical compound C1CC(C(=O)O)CCN1C(C=C1)=CC=C1NC1C2C(=O)NNCC2NC(C=2C=CC=CC=2)N1 CQYPQRMXAKUQDG-UHFFFAOYSA-N 0.000 claims 1
- GWYVDNLLCWVVLH-UHFFFAOYSA-N 1-[5-oxo-4-[4-(piperazin-1-ylmethyl)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidine-4-carboxylic acid Chemical compound C1CC(C(=O)O)CCN1C1=NC(NC=2C=CC(CN3CCNCC3)=CC=2)=C2C(=O)NN=CC2=N1 GWYVDNLLCWVVLH-UHFFFAOYSA-N 0.000 claims 1
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- RDRKXVZADSMSRV-UHFFFAOYSA-N 1-[[4-[[2-(4-cyanopiperidin-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]methyl]piperidine-4-carboxylic acid Chemical compound C1CC(C(=O)O)CCN1CC(C=C1)=CC=C1NC1=NC(N2CCC(CC2)C#N)=NC2=C1C(=O)NN=C2 RDRKXVZADSMSRV-UHFFFAOYSA-N 0.000 claims 1
- TYXUMIXYFXBMAE-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yl)-4-[4-(piperazin-1-ylmethyl)anilino]-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=C3OCOC3=CC=2)NC1NC(C=C1)=CC=C1CN1CCNCC1 TYXUMIXYFXBMAE-UHFFFAOYSA-N 0.000 claims 1
- GEIUOZVZDHABJA-UHFFFAOYSA-N 2-(4-ethylpiperazin-1-yl)-4-[4-(piperazin-1-ylmethyl)anilino]-6h-pyrimido[4,5-d]pyridazin-5-one;hydrochloride Chemical compound Cl.C1CN(CC)CCN1C1=NC(NC=2C=CC(CN3CCNCC3)=CC=2)=C2C(=O)NN=CC2=N1 GEIUOZVZDHABJA-UHFFFAOYSA-N 0.000 claims 1
- KFHYJLQWOOBWIW-UHFFFAOYSA-N 2-(4-methylpiperidin-1-yl)-4-[4-(2-piperazin-1-ylethoxy)anilino]-6h-pyrimido[4,5-d]pyridazin-5-one;hydrochloride Chemical compound Cl.C1CC(C)CCN1C1=NC(NC=2C=CC(OCCN3CCNCC3)=CC=2)=C2C(=O)NN=CC2=N1 KFHYJLQWOOBWIW-UHFFFAOYSA-N 0.000 claims 1
- IZJDDAXLNVWKQV-UHFFFAOYSA-N 2-(6-azaspiro[2.5]octan-6-yl)-4-(4-morpholin-4-ylanilino)-6h-pyrimido[4,5-d]pyridazin-5-one Chemical compound C=12C(=O)NN=CC2=NC(N2CCC3(CC3)CC2)=NC=1NC(C=C1)=CC=C1N1CCOCC1 IZJDDAXLNVWKQV-UHFFFAOYSA-N 0.000 claims 1
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- WGDFDNOMSGBBJS-UHFFFAOYSA-N 2-(azepan-1-yl)-4-[4-[2-(4-ethylpiperazin-1-yl)ethyl]anilino]-6h-pyrimido[4,5-d]pyridazin-5-one Chemical compound C1CN(CC)CCN1CCC(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 WGDFDNOMSGBBJS-UHFFFAOYSA-N 0.000 claims 1
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- ITORKKLKAZVJBF-UHFFFAOYSA-N 2-[1-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-4-yl]-2-methylpropanoic acid Chemical compound C1CC(C(C)(C)C(O)=O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 ITORKKLKAZVJBF-UHFFFAOYSA-N 0.000 claims 1
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- LENHGPBRXMASGO-UHFFFAOYSA-N 2-[1-[4-[[2-(azocan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-4-yl]acetic acid Chemical compound C1CC(CC(=O)O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCCC2)=NC2=C1C(=O)NN=C2 LENHGPBRXMASGO-UHFFFAOYSA-N 0.000 claims 1
- FUZONMXIBGUQPR-UHFFFAOYSA-N 2-[1-[4-[[2-[cyclohexyl(methyl)amino]-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-4-yl]acetic acid Chemical compound N=1C(NC=2C=CC(=CC=2)N2CCC(CC(O)=O)CC2)=C(C(NN=C2)=O)C2=NC=1N(C)C1CCCCC1 FUZONMXIBGUQPR-UHFFFAOYSA-N 0.000 claims 1
- AJXVRZSFKIWMPE-UHFFFAOYSA-N 2-[1-[4-[[6-(3-hydroxypiperidin-1-yl)pyridin-3-yl]amino]-5-oxo-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C1C(O)CCCN1C(N=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC2=C1C(=O)NN=C2 AJXVRZSFKIWMPE-UHFFFAOYSA-N 0.000 claims 1
- YBHNNEQRDMHSQQ-UHFFFAOYSA-N 2-[1-[4-[[6-(4-ethylpiperazin-1-yl)pyridin-3-yl]amino]-5-oxo-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C1CN(CC)CCN1C(N=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC2=C1C(=O)NN=C2 YBHNNEQRDMHSQQ-UHFFFAOYSA-N 0.000 claims 1
- KAZVWDLCKKDSPA-UHFFFAOYSA-N 2-[1-[4-[[6-(4-methylpiperazin-1-yl)pyridin-3-yl]amino]-5-oxo-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C1CN(C)CCN1C(N=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC2=C1C(=O)NN=C2 KAZVWDLCKKDSPA-UHFFFAOYSA-N 0.000 claims 1
- OOLXTNYZCCEZJE-UHFFFAOYSA-N 2-[1-[5-[(5-oxo-2-phenyl-6h-pyrimido[4,5-d]pyridazin-4-yl)amino]pyridin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(C=2C=CC=CC=2)=NC=1NC(C=N1)=CC=C1N1CCC(CC#N)CC1 OOLXTNYZCCEZJE-UHFFFAOYSA-N 0.000 claims 1
- OVBVNXVTONKYRW-UHFFFAOYSA-N 2-[1-[5-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]pyridin-2-yl]piperidin-4-yl]acetic acid Chemical compound C1CC(CC(=O)O)CCN1C(N=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 OVBVNXVTONKYRW-UHFFFAOYSA-N 0.000 claims 1
- SINXYUJLCYIKMA-UHFFFAOYSA-N 2-[1-[5-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]pyridin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCCCCC2)=NC=1NC(C=N1)=CC=C1N1CCC(CC#N)CC1 SINXYUJLCYIKMA-UHFFFAOYSA-N 0.000 claims 1
- AEWNGOHLUNPQEQ-UHFFFAOYSA-N 2-[1-[5-oxo-4-(3,4,5-trimethoxyanilino)-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound COC1=C(OC)C(OC)=CC(NC=2C=3C(=O)NN=CC=3N=C(N=2)N2CCC(CC#N)CC2)=C1 AEWNGOHLUNPQEQ-UHFFFAOYSA-N 0.000 claims 1
- AOMSNALEFNZLAY-UHFFFAOYSA-N 2-[1-[5-oxo-4-(4-piperazin-1-ylanilino)-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=C1)=CC=C1N1CCNCC1 AOMSNALEFNZLAY-UHFFFAOYSA-N 0.000 claims 1
- FJJYDXLMPWBGSK-UHFFFAOYSA-N 2-[1-[5-oxo-4-[(6-piperazin-1-ylpyridin-3-yl)amino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=N1)=CC=C1N1CCNCC1 FJJYDXLMPWBGSK-UHFFFAOYSA-N 0.000 claims 1
- RYGOOQDQGBYSJO-UHFFFAOYSA-N 2-[1-[5-oxo-4-[4-(2-piperazin-1-ylethoxy)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=C1)=CC=C1OCCN1CCNCC1 RYGOOQDQGBYSJO-UHFFFAOYSA-N 0.000 claims 1
- FRTDJFPREPWBPC-UHFFFAOYSA-N 2-[1-[5-oxo-4-[4-(2-piperidin-4-ylethoxy)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=C1)=CC=C1OCCC1CCNCC1 FRTDJFPREPWBPC-UHFFFAOYSA-N 0.000 claims 1
- ODNKDIDXPUIXMO-UHFFFAOYSA-N 2-[1-[5-oxo-4-[4-(3-piperazin-1-ylpropyl)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCC(CC#N)CC2)=NC=1NC(C=C1)=CC=C1CCCN1CCNCC1 ODNKDIDXPUIXMO-UHFFFAOYSA-N 0.000 claims 1
- BFUHTWSWTXIEJC-UHFFFAOYSA-N 2-[1-[5-oxo-4-[4-(piperazin-1-ylmethyl)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetic acid;hydrochloride Chemical compound Cl.C1CC(CC(=O)O)CCN1C1=NC(NC=2C=CC(CN3CCNCC3)=CC=2)=C2C(=O)NN=CC2=N1 BFUHTWSWTXIEJC-UHFFFAOYSA-N 0.000 claims 1
- QXCHIHIQFOYQGH-UHFFFAOYSA-N 2-[1-[5-oxo-4-[4-(trifluoromethoxy)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperidin-4-yl]acetonitrile Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC2=C1C(=O)NN=C2 QXCHIHIQFOYQGH-UHFFFAOYSA-N 0.000 claims 1
- CMPDWEQQDRGLNH-UHFFFAOYSA-N 2-[1-[[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]methyl]piperidin-4-yl]acetic acid Chemical compound C1CC(CC(=O)O)CCN1CC(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 CMPDWEQQDRGLNH-UHFFFAOYSA-N 0.000 claims 1
- VSJNCJFJORMKKU-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-(4-ethylpiperazin-1-yl)anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound C1CN(CC)CCN1C(C=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC(C=N)=C1C(N)=O VSJNCJFJORMKKU-UHFFFAOYSA-N 0.000 claims 1
- LOHLQMZDHKALKA-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[2-(4-ethylpiperazin-1-yl)ethyl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound C1CN(CC)CCN1CCC(C=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC(C=N)=C1C(N)=O LOHLQMZDHKALKA-UHFFFAOYSA-N 0.000 claims 1
- KTPXXXTUVSXPIH-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[2-[4-(2-hydroxyethyl)piperazin-1-yl]ethyl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1CCN1CCN(CCO)CC1 KTPXXXTUVSXPIH-UHFFFAOYSA-N 0.000 claims 1
- UYPKOPXCRRSNHM-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[2-[4-(hydroxymethyl)piperidin-1-yl]ethoxy]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1OCCN1CCC(CO)CC1 UYPKOPXCRRSNHM-UHFFFAOYSA-N 0.000 claims 1
- OXSCRKLUUHJBDL-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[4-(2,3-dihydroxypropyl)piperazin-1-yl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1N1CCN(CC(O)CO)CC1 OXSCRKLUUHJBDL-UHFFFAOYSA-N 0.000 claims 1
- OVQIQNNRBIZJJN-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[4-(2-hydroxy-2-methylpropanoyl)piperazin-1-yl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound C1CN(C(=O)C(C)(O)C)CCN1C(C=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC(C=N)=C1C(N)=O OVQIQNNRBIZJJN-UHFFFAOYSA-N 0.000 claims 1
- GQRWHUYOCWHVPM-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[4-(2-hydroxyethyl)piperidin-1-yl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1N1CCC(CCO)CC1 GQRWHUYOCWHVPM-UHFFFAOYSA-N 0.000 claims 1
- ATZFYVBJZLYNQV-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[4-[4-(3-hydroxypropyl)piperazin-1-yl]anilino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1N1CCN(CCCO)CC1 ATZFYVBJZLYNQV-UHFFFAOYSA-N 0.000 claims 1
- WWQRRHZTBFDFJY-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-[[6-[4-(2-diazenyl-2-iminoethyl)piperidin-1-yl]pyridin-3-yl]amino]-6-methanimidoylpyrimidine-5-carboxamide Chemical compound N1=C(N2CCC(CC#N)CC2)N=C(C=N)C(C(=O)N)=C1NC(C=N1)=CC=C1N1CCC(CC(=N)N=N)CC1 WWQRRHZTBFDFJY-UHFFFAOYSA-N 0.000 claims 1
- PMMAJXCZQPBWMB-UHFFFAOYSA-N 2-[4-(cyanomethyl)piperidin-1-yl]-4-methanimidoyl-6-[4-[4-(2-methoxyethyl)piperazin-1-yl]anilino]pyrimidine-5-carboxamide Chemical compound C1CN(CCOC)CCN1C(C=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC(C=N)=C1C(N)=O PMMAJXCZQPBWMB-UHFFFAOYSA-N 0.000 claims 1
- IKJGJDKBIUHBPU-UHFFFAOYSA-N 2-[4-(morpholin-4-ylmethyl)phenyl]-4-[4-(piperazin-1-ylmethyl)anilino]-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=CC(CN3CCOCC3)=CC=2)NC1NC(C=C1)=CC=C1CN1CCNCC1 IKJGJDKBIUHBPU-UHFFFAOYSA-N 0.000 claims 1
- FTUTYOPDMHSCDE-UHFFFAOYSA-N 2-[4-[4-[(5-oxo-2-phenyl-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]cyclohexyl]acetic acid Chemical compound C1CC(CC(=O)O)CCC1C(C=C1)=CC=C1NC1C2C(=O)NNCC2NC(C=2C=CC=CC=2)N1 FTUTYOPDMHSCDE-UHFFFAOYSA-N 0.000 claims 1
- RBSRPNFTFMGELL-UHFFFAOYSA-N 2-[4-[4-[(5-oxo-2-phenyl-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperazin-1-yl]acetic acid Chemical compound C1CN(CC(=O)O)CCN1C(C=C1)=CC=C1NC1C2C(=O)NNCC2NC(C=2C=CC=CC=2)N1 RBSRPNFTFMGELL-UHFFFAOYSA-N 0.000 claims 1
- FISOYMNWGMVMAG-UHFFFAOYSA-N 2-[4-[4-[(5-oxo-2-phenyl-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperidin-1-yl]acetic acid Chemical compound C1CN(CC(=O)O)CCC1C(C=C1)=CC=C1NC1C2C(=O)NNCC2NC(C=2C=CC=CC=2)N1 FISOYMNWGMVMAG-UHFFFAOYSA-N 0.000 claims 1
- CXXPNTGGRNQRLO-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenoxy]piperidin-1-yl]acetic acid Chemical compound C1CN(CC(=O)O)CCC1OC(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 CXXPNTGGRNQRLO-UHFFFAOYSA-N 0.000 claims 1
- RRPYHFCTYGYGDP-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]-2-methylpropanamide Chemical compound C1CN(C(C)(C)C(N)=O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 RRPYHFCTYGYGDP-UHFFFAOYSA-N 0.000 claims 1
- BUHQHAKCQJVJNR-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]-2-methylpropanenitrile Chemical compound C1CN(C(C)(C#N)C)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 BUHQHAKCQJVJNR-UHFFFAOYSA-N 0.000 claims 1
- PGWIMNRICNCIBR-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]-2-methylpropanoic acid Chemical compound C1CN(C(C)(C)C(O)=O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 PGWIMNRICNCIBR-UHFFFAOYSA-N 0.000 claims 1
- GYAKIFQKEUIRSB-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]acetic acid Chemical compound C1CN(CC(=O)O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 GYAKIFQKEUIRSB-UHFFFAOYSA-N 0.000 claims 1
- JAJPXOXMPWOKPD-UHFFFAOYSA-N 2-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCCCCC2)=NC=1NC(C=C1)=CC=C1N1CCN(CC#N)CC1 JAJPXOXMPWOKPD-UHFFFAOYSA-N 0.000 claims 1
- CHDJUUAJRMMYHT-UHFFFAOYSA-N 2-[4-[4-[[5-carbamoyl-2-[4-(cyanomethyl)piperidin-1-yl]-6-methanimidoylpyrimidin-4-yl]amino]phenyl]piperazin-1-yl]-2-methylpropanoic acid Chemical compound C1CN(C(C)(C)C(O)=O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCC(CC#N)CC2)=NC(C=N)=C1C(N)=O CHDJUUAJRMMYHT-UHFFFAOYSA-N 0.000 claims 1
- YKMKSKQQPHLCCJ-UHFFFAOYSA-N 2-[4-[5-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]pyridin-2-yl]piperazin-1-yl]acetic acid Chemical compound C1CN(CC(=O)O)CCN1C(N=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 YKMKSKQQPHLCCJ-UHFFFAOYSA-N 0.000 claims 1
- QEHHYYYDYIPNSU-UHFFFAOYSA-N 2-[4-[5-oxo-4-[4-(2-piperazin-1-ylethoxy)anilino]-6h-pyrimido[4,5-d]pyridazin-2-yl]piperazin-1-yl]acetonitrile Chemical compound C=12C(=O)NN=CC2=NC(N2CCN(CC#N)CC2)=NC=1NC(C=C1)=CC=C1OCCN1CCNCC1 QEHHYYYDYIPNSU-UHFFFAOYSA-N 0.000 claims 1
- YNBDBXIEAYCZCT-UHFFFAOYSA-N 2-[5-[4-[[2-(azepan-1-yl)-5-carbamoyl-6-methanimidoylpyrimidin-4-yl]amino]phenyl]tetrazol-2-yl]acetic acid Chemical compound N1=C(N2CCCCCC2)N=C(C=N)C(C(=O)N)=C1NC(C=C1)=CC=C1C=1N=NN(CC(O)=O)N=1 YNBDBXIEAYCZCT-UHFFFAOYSA-N 0.000 claims 1
- YZINQLLBHOCDGX-UHFFFAOYSA-N 2-methyl-2-[1-[4-[(5-oxo-2-phenyl-6h-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperidin-4-yl]propanenitrile Chemical compound C1CC(C(C)(C#N)C)CCN1C(C=C1)=CC=C1NC1=NC(C=2C=CC=CC=2)=NC2=C1C(=O)NN=C2 YZINQLLBHOCDGX-UHFFFAOYSA-N 0.000 claims 1
- ODGXBLJUBMENDM-UHFFFAOYSA-N 2-methyl-2-[1-[4-[(5-oxo-2-phenyl-6h-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperidin-4-yl]propanoic acid Chemical compound C1CC(C(C)(C)C(O)=O)CCN1C(C=C1)=CC=C1NC1=NC(C=2C=CC=CC=2)=NC2=C1C(=O)NN=C2 ODGXBLJUBMENDM-UHFFFAOYSA-N 0.000 claims 1
- FQXFKRRYNPIDCF-UHFFFAOYSA-N 2-morpholin-4-yl-4-[4-(piperazin-1-ylmethyl)anilino]-6h-pyrimido[4,5-d]pyridazin-5-one;hydrochloride Chemical compound Cl.C=12C(=O)NN=CC2=NC(N2CCOCC2)=NC=1NC(C=C1)=CC=C1CN1CCNCC1 FQXFKRRYNPIDCF-UHFFFAOYSA-N 0.000 claims 1
- BJTVZYGZPOJXBU-UHFFFAOYSA-N 2-phenyl-4-(4-piperazin-1-ylanilino)-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=CC=CC=2)NC1NC(C=C1)=CC=C1N1CCNCC1 BJTVZYGZPOJXBU-UHFFFAOYSA-N 0.000 claims 1
- LGHYCNLIBKDMJF-UHFFFAOYSA-N 2-phenyl-4-[4-(2-piperazin-1-ylethoxy)anilino]-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=CC=CC=2)NC1NC(C=C1)=CC=C1OCCN1CCNCC1 LGHYCNLIBKDMJF-UHFFFAOYSA-N 0.000 claims 1
- DEJRBJRLVAFXHD-UHFFFAOYSA-N 2-phenyl-4-[4-(piperazin-1-ylmethyl)anilino]-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=CC=CC=2)NC1NC(C=C1)=CC=C1CN1CCNCC1 DEJRBJRLVAFXHD-UHFFFAOYSA-N 0.000 claims 1
- OOAKALDEVQOXAU-UHFFFAOYSA-N 2-phenyl-4-[[1-(2-piperazin-1-ylethyl)pyrazol-4-yl]amino]-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-5-one Chemical compound C12C(=O)NNCC2NC(C=2C=CC=CC=2)NC1NC(=C1)C=NN1CCN1CCNCC1 OOAKALDEVQOXAU-UHFFFAOYSA-N 0.000 claims 1
- BTERNPAPFOIBIX-UHFFFAOYSA-N 3-[1-[4-[(5-oxo-2-phenyl-2,3,4,4a,6,7,8,8a-octahydro-1H-pyrimido[4,5-d]pyridazin-4-yl)amino]phenyl]piperidin-4-yl]propanoic acid Chemical compound C1CC(CCC(=O)O)CCN1C(C=C1)=CC=C1NC1C2C(=O)NNCC2NC(C=2C=CC=CC=2)N1 BTERNPAPFOIBIX-UHFFFAOYSA-N 0.000 claims 1
- LERGMBDKQPLVFB-UHFFFAOYSA-N 3-[1-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperidin-4-yl]propanoic acid Chemical compound C1CC(CCC(=O)O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 LERGMBDKQPLVFB-UHFFFAOYSA-N 0.000 claims 1
- UJXAOIWSKTYNIE-UHFFFAOYSA-N 3-[4-[4-[[2-(azepan-1-yl)-5-oxo-6h-pyrimido[4,5-d]pyridazin-4-yl]amino]phenyl]piperazin-1-yl]-3-oxopropanenitrile Chemical compound C1CN(C(CC#N)=O)CCN1C(C=C1)=CC=C1NC1=NC(N2CCCCCC2)=NC2=C1C(=O)NN=C2 UJXAOIWSKTYNIE-UHFFFAOYSA-N 0.000 claims 1
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
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- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Oncology (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562263398P | 2015-12-04 | 2015-12-04 | |
| US62/263,398 | 2015-12-04 | ||
| PCT/US2016/064178 WO2017095898A1 (en) | 2015-12-04 | 2016-11-30 | Uses of pyrimido-pyrimidazinones to treat cancer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2018535995A true JP2018535995A (ja) | 2018-12-06 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| JP2018528583A Pending JP2018535995A (ja) | 2015-12-04 | 2016-11-30 | 癌を治療するためのピリミド−ピリダジノンの使用 |
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| Country | Link |
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| US (2) | US10188654B2 (es) |
| EP (1) | EP3383399A1 (es) |
| JP (1) | JP2018535995A (es) |
| KR (1) | KR20180084983A (es) |
| CN (1) | CN108601785A (es) |
| AR (1) | AR106830A1 (es) |
| AU (1) | AU2016365215A1 (es) |
| BR (1) | BR112018011196A2 (es) |
| CA (1) | CA3006762A1 (es) |
| IL (1) | IL259781A (es) |
| MX (1) | MX2018006776A (es) |
| RU (1) | RU2018124289A (es) |
| TW (1) | TW201726141A (es) |
| WO (1) | WO2017095898A1 (es) |
| ZA (1) | ZA201803593B (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN103974955B (zh) * | 2011-08-23 | 2018-06-19 | 阿萨纳生物科技有限责任公司 | 嘧啶并-哒嗪酮化合物及其用途 |
| KR20190140011A (ko) | 2017-04-28 | 2019-12-18 | 아사나 바이오사이언시스 엘엘씨 | 아토피성 피부염을 치료하고, 활성 약학적 성분의 안정성을 개선하기 위한 제형물, 방법, 키트, 및 투여형 |
| CN111961035B (zh) * | 2019-05-20 | 2022-11-01 | 南京科技职业学院 | 一类含有羟基异喹啉类结构的化合物、药物组合物以及其应用 |
| CN118974051A (zh) * | 2022-03-22 | 2024-11-15 | 上海维申医药有限公司 | 作为Toll样受体激动剂的嘧啶并哒嗪酮类化合物 |
| WO2025020171A1 (en) * | 2023-07-27 | 2025-01-30 | Libertas Bio, Inc. | Crystalline forms of a jak/syk inhibitor |
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| KR101623997B1 (ko) * | 2008-04-16 | 2016-05-24 | 포톨라 파마슈티컬스, 인코포레이티드 | syk 또는 JAK 키나제 억제제로서의 2,6-디아미노-피리미딘-5-일-카르복스아미드 |
| WO2010019637A1 (en) | 2008-08-12 | 2010-02-18 | Smithkline Beecham Corporation | Chemical compounds |
| US8404677B2 (en) | 2009-10-29 | 2013-03-26 | Genosco | Kinase inhibitors |
| US8796289B2 (en) * | 2011-07-19 | 2014-08-05 | Abbvie Inc. | Pyridazino[4,5-D]pyrimidin-5(6H)-one inhibitors of kinases |
| CN103974955B (zh) * | 2011-08-23 | 2018-06-19 | 阿萨纳生物科技有限责任公司 | 嘧啶并-哒嗪酮化合物及其用途 |
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2016
- 2016-11-25 AR ARP160103628A patent/AR106830A1/es unknown
- 2016-11-28 TW TW105138865A patent/TW201726141A/zh unknown
- 2016-11-30 CN CN201680081107.0A patent/CN108601785A/zh active Pending
- 2016-11-30 CA CA3006762A patent/CA3006762A1/en not_active Abandoned
- 2016-11-30 MX MX2018006776A patent/MX2018006776A/es unknown
- 2016-11-30 RU RU2018124289A patent/RU2018124289A/ru not_active Application Discontinuation
- 2016-11-30 JP JP2018528583A patent/JP2018535995A/ja active Pending
- 2016-11-30 US US15/365,222 patent/US10188654B2/en active Active
- 2016-11-30 BR BR112018011196A patent/BR112018011196A2/pt not_active IP Right Cessation
- 2016-11-30 AU AU2016365215A patent/AU2016365215A1/en not_active Abandoned
- 2016-11-30 EP EP16813264.5A patent/EP3383399A1/en not_active Withdrawn
- 2016-11-30 KR KR1020187017697A patent/KR20180084983A/ko not_active Withdrawn
- 2016-11-30 WO PCT/US2016/064178 patent/WO2017095898A1/en not_active Ceased
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2018
- 2018-05-30 ZA ZA2018/03593A patent/ZA201803593B/en unknown
- 2018-06-03 IL IL259781A patent/IL259781A/en unknown
- 2018-11-02 US US16/179,274 patent/US20190070182A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| TW201726141A (zh) | 2017-08-01 |
| ZA201803593B (en) | 2019-04-24 |
| AU2016365215A1 (en) | 2018-07-05 |
| US10188654B2 (en) | 2019-01-29 |
| EP3383399A1 (en) | 2018-10-10 |
| US20190070182A1 (en) | 2019-03-07 |
| CN108601785A (zh) | 2018-09-28 |
| IL259781A (en) | 2018-07-31 |
| CA3006762A1 (en) | 2017-06-08 |
| AR106830A1 (es) | 2018-02-21 |
| KR20180084983A (ko) | 2018-07-25 |
| WO2017095898A1 (en) | 2017-06-08 |
| RU2018124289A (ru) | 2020-01-14 |
| MX2018006776A (es) | 2018-08-15 |
| BR112018011196A2 (pt) | 2018-11-21 |
| US20170157126A1 (en) | 2017-06-08 |
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